Basciano Heather, Miller Abigale, Baker Chris, Naples Mark, Adeli Khosrow
Molecular Structure and Function, Research Institute, The Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Am J Physiol Gastrointest Liver Physiol. 2009 Aug;297(2):G323-32. doi: 10.1152/ajpgi.90546.2008. Epub 2009 Jun 4.
Liver X receptor-alpha (LXRalpha) is considered a master regulator of hepatic lipid metabolism; however, little is known about the link between LXR activation, hepatic insulin signaling, and very low-density lipoprotein (VLDL)-apolipoprotein B (apoB) assembly and secretion. Here, we examined the effect of LXRalpha activation on hepatic insulin signaling and apoB-lipoprotein production. In vivo activation of LXRalpha for 7 days using a synthetic LXR agonist, TO901317, in hamsters led to increased plasma triglyceride (TG; 3.6-fold compared with vehicle-treated controls, P = 0.006), apoB (54%, P < 0.0001), and VLDL-TG (eightfold increase compared with vehicle). As expected, LXR stimulation activated maturation of sterol response element binding protein-1c (SREBP-1c) as well as the SREBP-1c target genes steroyl CoA desaturase (SCD) and fatty acid synthase (FAS). Metabolic pulse-chase labeling experiments in primary hamster hepatocytes showed increased stability and secretion of newly synthesized apoB following LXR activation. Microsomal triglyceride transfer protein (MTP) mRNA and protein were unchanged, however, likely because of the relatively short period of treatment and long half-life of MTP mRNA. Examination of hepatic insulin-signaling molecules revealed LXR-mediated reductions in insulin receptor (IR)beta subunit mass (39%, P = 0.014) and insulin receptor substrate (IRS)-1 tyrosine phosphorylation (24%, P = 0.023), as well as increases in protein tyrosine phosphatase (PTP)1B (29%, P < 0.001) protein mass. In contrast to IRS-1, a twofold increase in IRS-2 mass (228%, P = 0.0037) and a threefold increase in IRS-2 tyrosine phosphorylation (321%, P = 0.012) were observed. In conclusion, LXR activation dysregulates hepatic insulin signaling and leads to a considerable increase in the number of circulating TG-rich VLDL-apoB particles, likely due to enhanced hepatic assembly and secretion of apoB-containing lipoproteins.
肝脏X受体α(LXRα)被认为是肝脏脂质代谢的主要调节因子;然而,关于LXR激活、肝脏胰岛素信号传导以及极低密度脂蛋白(VLDL)-载脂蛋白B(apoB)组装与分泌之间的联系,人们所知甚少。在此,我们研究了LXRα激活对肝脏胰岛素信号传导和apoB-脂蛋白产生的影响。在仓鼠体内使用合成LXR激动剂TO901317激活LXRα 7天,导致血浆甘油三酯(TG;与载体处理的对照组相比增加3.6倍,P = 0.006)、apoB(增加54%,P < 0.0001)和VLDL-TG(与载体相比增加8倍)升高。正如预期的那样,LXR刺激激活了固醇调节元件结合蛋白-1c(SREBP-1c)的成熟以及SREBP-1c靶基因固醇辅酶A去饱和酶(SCD)和脂肪酸合酶(FAS)。原代仓鼠肝细胞中的代谢脉冲追踪标记实验表明,LXR激活后新合成的apoB的稳定性和分泌增加。然而,微粒体甘油三酯转移蛋白(MTP)的mRNA和蛋白未发生变化,这可能是由于处理时间相对较短以及MTP mRNA的半衰期较长。对肝脏胰岛素信号分子的检测显示,LXR介导胰岛素受体(IR)β亚基质量降低(39%,P = 0.014)以及胰岛素受体底物(IRS)-1酪氨酸磷酸化降低(24%,P = 0.023),同时蛋白酪氨酸磷酸酶(PTP)1B蛋白质量增加(29%,P < 0.001)。与IRS-1相反,观察到IRS-2质量增加两倍(228%,P = 0.0037)以及IRS-2酪氨酸磷酸化增加三倍(321%,P = 0.012)。总之,LXR激活会使肝脏胰岛素信号传导失调,并导致循环中富含TG的VLDL-apoB颗粒数量显著增加,这可能是由于肝脏中含apoB脂蛋白的组装和分泌增强所致。
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